Logan R A, Bhogal B, Das A K, McKee P M, Black M M
United Medical Schools of Guy's Hospital, London, U.K.
Br J Dermatol. 1987 Oct;117(4):471-8. doi: 10.1111/j.1365-2133.1987.tb04927.x.
We have re-examined the site of deposition of IgG anti-basement membrane zone antibodies in 228 sera from suspected cases of bullous pemphigoid (BP), using 1.0 M sodium chloride split-skin as substrate for indirect immunofluorescence. Nine sera (4%) produced fluorescence on the floor of the split suggesting sub-basal lamina antibody deposition compatible with a diagnosis of epidermolysis bullosa acquisita (EBA). This ultrastructural localization was confirmed in only three of these nine by immuno-electron microscopy. Clinical details were available on six of these nine cases, and none had clinical features suggesting EBA. We have found the split-skin immunofluorescence technique unhelpful in identifying 'missed' cases of EBA. The prevalence of EBA presenting as BP would appear to be very low indeed in the U.K.
我们使用1.0M氯化钠分离皮肤作为间接免疫荧光的底物,重新检查了228份来自疑似大疱性类天疱疮(BP)病例血清中IgG抗基底膜带抗体的沉积部位。9份血清(4%)在分离皮肤的底层产生荧光,提示基底膜下抗体沉积,符合获得性大疱性表皮松解症(EBA)的诊断。这9例中只有3例通过免疫电子显微镜证实了这种超微结构定位。这9例中有6例有临床细节,且均无提示EBA的临床特征。我们发现分离皮肤免疫荧光技术无助于识别“漏诊”的EBA病例。在英国,表现为BP的EBA患病率似乎确实非常低。